Histiocytosis in a 7 year old boy, a diagnostic dilemma.

Authors

  • Okpokowuruk FS Department of Paediatrics
  • Umana IN Department of Pathology
  • Adesina OA Department of Paediatrics

Abstract

Abstract: Histiocytoses are a group of rare disorders which are characterized by the infiltration/ accumulation of histiocytic cells in affected tissues. Their mode of clinical presentation varies greatly and can represent a diagnostic challenge in our environment where there is a paucity of diagnostic facilities. This report is on a 7 year old boy with probable Histiocytosis who initially presented with signs and symptoms suggestive of pulmonary tuberculosis. Difficulties in reaching a conclusive diagnosis of the type of histiocytosis coupled with financial limitations contributed to the eventual demise of this patient.

Keywords: Histiocytosis, tuberculosis, diagnostic facilities

Published

2024-07-02

Issue

Vol. 40 No. 1 (2013): Nigerian Journal of Paediatrics

Section

CASE REPORTS

License

This is an open-access journal, and articles are distributed under the terms of the Creative Commons Attribution 4.0 License, which allows others to remix, transform, and build upon the work even, commercially, as long as appropriate credit is given to the author, and the new creations are licensed under identical terms

How to Cite

Histiocytosis in a 7 year old boy, a diagnostic dilemma. (2024). NIGERIAN JOURNAL OF PAEDIATRICS, 40(1), 91-92. https://www.njpaediatrics.com/index.php/njp/article/view/404